Canonical Allele Identifier: CA405418784

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220901G>A (hg19) ; chr19:g.35730000G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730000G>A , CM000681.2:g.35730000G>A	GRCh38
NC_000019.9:g.36220901G>A , CM000681.1:g.36220901G>A	GRCh37
NC_000019.8:g.40912741G>A	NCBI36
NG_052906.1:g.16982G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4885G>A	ENSP00000501283.1:p.Val1629Met
ENST00000674114.2:c.2492G>A	ENSP00000501039.2:n.2492G>A
ENST00000684977.1:c.169G>A	ENSP00000509384.1:p.Val57Met
ENST00000685168.1:c.377G>A
ENST00000689544.1:n.104G>A
ENST00000691421.1:c.172G>A	ENSP00000508674.1:p.Val58Met
ENST00000691855.1:c.4493G>A
ENST00000692961.1:c.4951G>A	ENSP00000509289.1:p.Val1651Met
ENST00000420124.4:c.4951G>A MANE Select	ENSP00000398837.2:p.Val1651Met
ENST00000673918.1:c.4885G>A	ENSP00000501283.1:p.Val1629Met
ENST00000674114.1:c.2273G>A
ENST00000420124.2:c.4951G>A	ENSP00000398837.1:p.Val1651Met
NM_014727.2:c.4951G>A	NP_055542.1:p.Val1651Met
XM_011527561.1:c.4885G>A	XP_011525863.1:p.Val1629Met
XM_011527562.1:c.4951G>A	XP_011525864.1:p.Val1651Met
XM_011527563.1:c.4675G>A	XP_011525865.1:p.Val1559Met
XM_011527561.2:c.4387G>A	XP_011525863.2:p.Val1463Met
XM_011527562.2:c.4951G>A	XP_011525864.1:p.Val1651Met
XM_017027544.1:c.4951G>A	XP_016883033.1:p.Val1651Met
XM_017027545.1:c.4387G>A	XP_016883034.1:p.Val1463Met
XM_017027546.1:c.1915G>A	XP_016883035.1:p.Val639Met
NM_014727.3:c.4951G>A MANE Select	NP_055542.1:p.Val1651Met